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ANVISA registration and regulatory affairs

We run the full process with ANVISA — at the pace the registration and certification process allows, with complete transparency.

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ANVISA registration and regulatory affairs 04 SOLUTION · SETFREE
WHAT IT INCLUDES

The complete regulatory cycle

01 Technical dossier and submission
02 Registration, renewal and maintenance
03 AFE, authorizations and regularized importation
04 Post-market surveillance
WHO IT IS FOR

For those who need their registration in order

Foreign manufacturers

They need a Brazilian registration holder to place the product on the market.

Registration holders

They have a registration expiring, a change of scope or an open issue to resolve.

Importers

They need AFE, authorizations and importation within the rules.

HOW IT STARTS

Three steps from first contact

01

Diagnostic conversation

You tell us the context and the constraint; we say plainly whether it is something we do.

02

Scope and proposal

Written scope, responsibilities and what depends on third parties — no hidden steps.

03

Execution with follow-up

A single point of contact and status you can check — a word that holds.

Send us whatever dossier you already have.

Send the context — we answer with what is real, in the time it takes.

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